Sr Principal Engineer, Acute Disposables

7 days ago

Bengaluru, India Baxter Full time

Vantive: A New Company Built On Our Legacy

Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.

At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us are driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support.

*Completion of the proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions.

About Baxter

Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter’s employees worldwide are building upon the company’s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care.

Job Description 

Responsible for developing solutions to challenging issues associated with the design, development, and sustenance engineering for our new and existing Disposables for the Acute Therapies product portfolio. Independently drive/contribute to the Projects/Initiatives involving Engineering change management, solutions for Product quality issues, root cause analysis, NCR handling, CAPAs, verification & validation, design transfer, Value improvement programs and Regulatory compliance activities. Contribute to the development of new functions/features to be integrated into the existing products/new products. 

Essential Duties and Responsibilities:


 Education and Experience

Graduate or Postgraduate in Mechanical Engineering/Bio Medical engineering or Equivalent.
Minimum 8 years of R&D experience in New product development/Sustenance.
Prior experience of Medical Device Risk management activities.
A proven track record of management/leadership effectiveness in a fast-paced environment.
Proven ability to create results within budget, timeline, and product/project deliverables.


A Career That Matters

innovation to meet the needs of the millions of people worldwide who depend on our medically necessary therapies and

technologies. We focus on increasing access to healthcare, innovating in crucial areas of unmet need, and pursuing

creative collaborations that bring our mission to life for patients every day.

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